| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033796-19033925 | Common:1; Rare:36 | ||||
| chr19:19105718-19105754 | Rare:13; Clinvar (pathogenic):1 | ||||
| chr19:19192110-19192212 | Common:1; Rare:35 | ||||
| chr19:19192582-19192955 | Common:2; Rare:98 | ||||
| chr19:19266493-19266950 | Common:3; Rare:107 | ||||
| chr19:19320464-19320858 | Common:4; Rare:151 | ||||
| chr19:19385892-19386090 | Rare:71 | ||||
| chr19:19516157-19516277 | Rare:71; Clinvar (pathogenic):1 | ||||
| chr19:19663488-19663729 | Rare:83 | ||||
| chr19:19821662-19821905 | Common:1; Rare:81 | ||||
| chr19:29213114-29213307 | Common:3; Rare:62 | ||||
| chr19:29606166-29606321 | Rare:50 | ||||
| chr19:29665250-29665456 | Common:4; Rare:74 | ||||
| chr19:29715047-29715312 | Common:1; Rare:99 | ||||
| chr19:32405541-32405808 | Rare:116 |